Abstract

BackgroundThe administrative process associated with clinical trial activation has been criticized as costly, complex, and time-consuming. Prior research has concentrated on identifying administrative barriers and proposing various solutions to reduce activation time, and consequently associated costs. Here, we expand on previous research by incorporating social network analysis and discrete-event simulation to support process improvement decision-making.MethodsWe searched for all operational data associated with the administrative process of activating industry-sponsored clinical trials at the Office of Clinical Research of the University of South Florida in Tampa, Florida. We limited the search to those trials initiated and activated between July 2011 and June 2012. We described the process using value stream mapping, studied the interactions of the various process participants using social network analysis, and modeled potential process modifications using discrete-event simulation.ResultsThe administrative process comprised 5 sub-processes, 30 activities, 11 decision points, 5 loops, and 8 participants. The mean activation time was 76.6 days. Rate-limiting sub-processes were those of contract and budget development. Key participants during contract and budget development were the Office of Clinical Research, sponsors, and the principal investigator. Simulation results indicate that slight increments on the number of trials, arriving to the Office of Clinical Research, would increase activation time by 11 %. Also, incrementing the efficiency of contract and budget development would reduce the activation time by 28 %. Finally, better synchronization between contract and budget development would reduce time spent on batching documentation; however, no improvements would be attained in total activation time.ConclusionThe presented process improvement analytic framework not only identifies administrative barriers, but also helps to devise and evaluate potential improvement scenarios. The strength of our framework lies in its system analysis approach that recognizes the stochastic duration of the activation process and the interdependence between process activities and entities.Electronic supplementary materialThe online version of this article (doi:10.1186/s13063-016-1227-2) contains supplementary material, which is available to authorized users.

Highlights

  • The administrative process associated with clinical trial activation has been criticized as costly, complex, and time-consuming

  • As explained in the results section, we have identified five sub-processes: Initial Preparation; Contract Negotiation; Budget Negotiation; Preparation for Western Institutional Review Board submission; and Final Preparation, which includes the final approvals by the principal investigator (PI), the University of South Florida (USF)’s Division of Sponsored Research and the trial sponsor

  • A total of 69 trials were excluded from time stamp extraction due to having missing data (n = 16), being still in process (n = 52), or because they were terminated for reasons beyond the scope of this study (n = 1)

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Summary

Introduction

The administrative process associated with clinical trial activation has been criticized as costly, complex, and time-consuming. This sizable amount is exonerated if we consider that the administrative process associated with trial activation in academic medical settings includes up to 30 different activities, involves up to 11 participants, and lasts on average, from 44 to 172 days [6, 8, 17, 18] Such complexity translates into delayed trial activation, which affects patient enrollment goals [19, 20] and diminishes the usefulness of trials by failing to attain evidence of investigated interventions on time [21]

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